ClearanceBrief
510(k) K000894 ยท EBG Crown And Bridge, Temporary, Resin

C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MO

ApplicantDental Ventures of America, Inc., Corona CA, US
DecisionSubstantially Equivalent, May 19, 2000
ReceivedMar 20, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K000894

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.